| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:31094725-31095050 | Rare:87; Clinvar:1 | ||||
| chr16:31108282-31108465 | Rare:41 | ||||
| chr16:31202626-31202879 | Common:2; Rare:89 | ||||
| chr16:31471931-31472186 | Rare:58 | ||||
| chr16:31508374-31508464 | Common:1; Rare:33 | ||||
| chr16:46689131-46689416 | Common:1; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46689509-46689708 | Common:2; Rare:83; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46973604-46973786 | Rare:84 | ||||
| chr16:47461035-47461374 | Common:2; Rare:129; Clinvar (benign):2 | ||||
| chr16:48365873-48366140 | Common:5; Rare:76 | ||||
| chr16:50266422-50266569 | Common:1; Rare:42 | ||||
| chr16:50693509-50693600 | Rare:37 | ||||
| chr16:53054875-53055068 | Common:1; Rare:43 | ||||
| chr16:53208305-53208500 | Rare:41 | ||||
| chr16:53703821-53704194 | Rare:111; Clinvar:4; Clinvar (benign):1 |